Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,639 recalls have been distributed to District of Columbia in the last 12 months.
Showing 4321–4340 of 27,451 recalls
Recalled Item: LifeVentEVO2 Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aeris EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo O2 Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy EV300 Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Garbin EVO Recalled by Philips Respironics, Inc. Due to Potential for sudden...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trilogy Evo Recalled by Philips Respironics, Inc. Due to Potential for...
The Issue: Potential for sudden loss of ventilation due to Battery Depleted or Loss of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 7 OR Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Interact Discovery RT Recalled by GE Medical Systems, SCS Due...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 5 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 7 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 6 Recalled by GE Medical Systems, SCS Due to GE...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Allia IGS 5 Pulse Recalled by GE Medical Systems, SCS Due to...
The Issue: GE HealthCare has become aware of the potential that adhesive material might...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LightStrike Blackout Curtains Recalled by XENEX Disinfection Services Inc....
The Issue: Blackout curtains are no longer recommended as a protective barrier against...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PERLA TL 25D SCREW 45 25-S TLF-DS 45 Recalled by SPINEART SA Due to Due to...
The Issue: Due to receiving information regarding difficulties with the insertion of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter Seprafilm Adhesion Barrier 1 Half Sheet Recalled by Baxter Healthcare...
The Issue: Product was distributed in the United States without proper regulatory approval.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision HSI Chronic Catheter Sport Pack 14.5 Fr/Ch (4.8mm)...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Various Alcon Custom Paks Surgical Procedure Pack containing Oasis 27Ga...
The Issue: Due to complaints of particulates, residue, occlusions, and bent tips for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palindrome Precision H Chronic Catheter Kit 14.5 Fr/Ch (4.8mm) x Recalled by...
The Issue: Products may not be heparin coated as indicated on the label-leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sterile convenience kits: a. Medline Retrograde PK-22025203-LF Recalled by...
The Issue: Surgical convenience kits containing Pure Pouch component that has weak...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.